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FDA 510(k)

ENVOY

K-Number: K022168 · 2002-08-01

Decision Date2002-08-01
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ENVOY is the device name listed in this FDA 510(k) record. The listed applicant is Mennen Medical , Ltd.. It received FDA 510(k) clearance on 2002-08-01 under 510(k) number K022168. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENVOY?

ENVOY is a medical device that received FDA 510(k) clearance on 2002-08-01. The listed applicant is Mennen Medical , Ltd.. The 510(k) number is K022168.

When did ENVOY receive FDA 510(k) clearance?

ENVOY received FDA 510(k) clearance on 2002-08-01, under 510(k) number K022168.

Who is the listed applicant for ENVOY?

The FDA 510(k) record lists Mennen Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENVOY?

The FDA product code for ENVOY is DQA.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Mennen Medical , Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 20 devices →

Related Devices (Code: DQA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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